“…XRD patterns of as-prepared SnO 2 , SG-E and SG-C were displayed in Fig [27,28]. According to Scherrer equation D=kλ/(βcosθ), where D is the crystallize size, k is a dimensionless shape factor (0.89), λ is the X-ray wavelength (0.15406 nm), β is the full width half the maximum intensity in radians and θ is the Bragg angle, the calculated mean crystallize size was 13nm.…”
“…XRD patterns of as-prepared SnO 2 , SG-E and SG-C were displayed in Fig [27,28]. According to Scherrer equation D=kλ/(βcosθ), where D is the crystallize size, k is a dimensionless shape factor (0.89), λ is the X-ray wavelength (0.15406 nm), β is the full width half the maximum intensity in radians and θ is the Bragg angle, the calculated mean crystallize size was 13nm.…”
“…29) (SnO 2 prepared by a melt-spinning and room temperature dealloying method), which once displayed better photocatalytic performance compared with other SnO 2 materials synthesized by spinning–dealloying, 29 commercial SnO 2 , 29 and literature notable SnO 2 -based photocatalysts. 48–50 These results suggest that the milling–dealloying method is a more effective method for fabricating higher activity nano-SnO 2 . Furthermore, it was noteworthy that SnO 2 -300 was superior to SnO 2 -150 (the 1.5 h RhB degradation rates were 90.06% and 86.20% for SnO 2 -300 and SnO 2 -150, respectively).…”
Compared with Cu50Sn50 prepared by ball milling at 150 r min−1, Cu50Sn50 prepared at 300 r min−1 exposes more active facts in η-Cu6Sn5, thus leading to a shorter dealloying time, smaller particle sizes, and higher degradation activity of nano-SnO2.
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